EP0778255A1 - Verfahren zur Herstellung der Akrylsäure - Google Patents

Verfahren zur Herstellung der Akrylsäure Download PDF

Info

Publication number
EP0778255A1
EP0778255A1 EP96308837A EP96308837A EP0778255A1 EP 0778255 A1 EP0778255 A1 EP 0778255A1 EP 96308837 A EP96308837 A EP 96308837A EP 96308837 A EP96308837 A EP 96308837A EP 0778255 A1 EP0778255 A1 EP 0778255A1
Authority
EP
European Patent Office
Prior art keywords
acrylic acid
weight
tower
aqueous
azeotropic distillation
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP96308837A
Other languages
English (en)
French (fr)
Other versions
EP0778255B1 (de
Inventor
Kazuhiko Sakamoto
Sei Nakahara
Takahiro Takeda
Masatoshi Ueoka
Yohji Akazawa
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Shokubai Co Ltd
Original Assignee
Nippon Shokubai Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nippon Shokubai Co Ltd filed Critical Nippon Shokubai Co Ltd
Publication of EP0778255A1 publication Critical patent/EP0778255A1/de
Application granted granted Critical
Publication of EP0778255B1 publication Critical patent/EP0778255B1/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
    • C07C57/02—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
    • C07C57/03—Monocarboxylic acids
    • C07C57/04—Acrylic acid; Methacrylic acid
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42—Separation; Purification; Stabilisation; Use of additives
    • C07C51/43—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation
    • C07C51/44—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation by distillation
    • C07C51/46—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation by distillation by azeotropic distillation

Definitions

  • the present invention relates to a process for producing acrylic acid at a high purity by separating by-products, particularly acetic acid efficiently from a mixed gas obtained by subjecting propylene and/or acrolein to catalytic gas-phase oxidation with a molecular oxygen-containing gas. More particularly, the present invention relates to a process for producing high-purity acrylic acid by contacting said mixed gas with an aqueous solution containing acrylic acid, acetic acid and a poorly-soluble-in-water solvent, to form an aqueous acrylic acid solution, and then subjecting the aqueous acrylic acid solution to azeotropic distillation in the presence of a poorly-soluble-in-water solvent to remove by-products.
  • a mixed gas containing acrylic acid (an intended compound) and by-products e.g. acetic acid
  • a mixed gas obtained by the catalytic gas-phase oxidation is absorbed by water in an acrylic acid-collecting tower to obtain an aqueous solution containing acrylic acid and by-products (e.g. acetic acid), followed by distillation of the aqueous solution for separation of acrylic acid and subsequent purification of the separated acrylic acid to obtain a product.
  • Japanese Patent Application Kokai (Laid-Open) No. 246941/1993 discloses a process in which the acetic acid solution obtained is circulated for reuse as an absorbent in the acrylic acid-collecting tower.
  • a solvent soluble in water in a non-negligible amount is used as a solvent for azeotropic distillation, a step is necessary for recovery of the solvent from the aqueous phase distilled off from the azeotropic distillation tower, requiring, besides the azeotropic distillation tower, a distillation tower for recovery of the solvent.
  • the acetic acid solution circulated for reuse as an absorbent contains no solvent and substantially no acrylic acid, the collection efficiency in the acrylic acid-collecting tower is insufficient.
  • Japanese Patent Publication No. 34691/1971 discloses a process which uses heptane as a solvent for azeotropic distillation.
  • the aqueous phase distilled off from the azeotropic distillation tower contains acrylic acid in an amount of only 0.5% by weight or less and, moreover, there is no description on the circulation of the aqueous phase for reuse.
  • the separation of acetic acid and water at the tower bottom is insufficient, making it difficult to obtain a high-purity acrylic acid product.
  • the object of the present invention lies in providing a high-quality acrylic acid product which has been unobtainable with conventional processes, by, in the production of acrylic acid by catalytic gas-phase oxidation of propylene and/or acrolein, treating the mixed gas formed by the catalytic gas-phase oxidation, by a noble method.
  • the present invention provides a process for production of acrylic acid, which comprises:
  • the present invention also provides, as one preferred embodiment of the above process, a process wherein the above-mentioned aqueous phase separated in the storage tank is circulated into the acrylic acid-collecting tower to use it as an acrylic acid-collecting agent.
  • acrylic acid can be collected at a high efficiency by introducing, into an acrylic acid-collecting tower, a mixed gas obtained by catalytic gas-phase oxidation of propylene and/or acrolein with a molecular oxygen-containing gas; and by subjecting the aqueous acrylic acid solution obtained by the above collection, to azeotropic distillation in an azeotropic distillation tower, a high-purity acrylic acid product can be obtained from the bottom of the distillation tower.
  • Fig. 1 which is an accompanying drawing, is a flow sheet showing a typical embodiment of the present invention. The present invention is hereinafter described specifically referring to Fig. 1.
  • the mixed gas containing acrylic acid and by-products (e.g. acetic acid), obtained by catalytic gas-phase oxidation of propylene and/or acrolein with a molecular oxygen-containing gas in the presence of an oxidation catalyst, is introduced into an acrylic acid-collecting tower 101 through a line 1, and is contacted with an aqueous collecting agent containing acrylic acid, acetic acid and a poorly-soluble-in-water solvent, introduced into the tower 101 through a line 2, to form an aqueous acrylic acid solution containing acrylic acid and by-products (e.g. acetic acid).
  • the mixed gas after contact with the aqueous collecting agent leaves the acrylic acid-collecting tower 101 through a line 3, and is recycled into an oxidation reaction step or discharged into the atmosphere as a waste gas via a combustion step.
  • the distilled mixture is introduced into a storage tank 10 through the line 6 and separated therein into (1) an organic phase composed substantially of the solvent alone and (2) an aqueous phase containing acrylic acid, acetic acid, the poorly-soluble-in-water solvent and water.
  • the organic phase is circulated into the azeotropic distillation tower 102 through the line 5.
  • the distilled mixture is allowed to stay in the storage tank 10 for 0.5-2 hours for complete separation of the organic phase and the aqueous phase.
  • the aqueous phase separated in the storage tank 10 is preferably circulated into the acrylic acid-collecting tower 101 through the line 2 to be used as an acrylic acid-collecting agent.
  • part of the aqueous phase may be discharged out of the system through a line 8.
  • the mixed gas introduced into the acrylic acid-collecting tower 101 i.e. the mixed gas obtained by catalytic gas-phase oxidation of propylene and/or acrolein with a molecular oxygen-containing gas, preferably contains acrylic acid, acetic acid and steam in amounts of 10-20% by weight, 0.2-1.0% by weight and 5-15% by weight, respectively.
  • acrylic acid, acetic acid and steam in amounts of 10-20% by weight, 0.2-1.0% by weight and 5-15% by weight, respectively.
  • the aqueous acrylic acid solution generally contains 50-80% by weight of acrylic acid, 1-5% by weight of acetic acid and 20-40% by weight of water under the ordinary conditions of acrylic acid synthesis.
  • the proportions of these components in the aqueous acrylic acid solution are not restricted to the above ranges and vary depending upon the operating conditions of the oxidation reactor and/or the acrylic acid-collecting tower.
  • the aqueous collecting agent used in the acrylic acid-collecting tower 101 must contain acrylic acid, acetic acid and a poorly-soluble-in-water solvent in amounts of 0.5-5.0% by weight, 3.0-10.0% by weight and 0.01-0.5% by weight, respectively.
  • An aqueous collecting agent containing 1.0-2.0% by weight of acrylic acid, 4.0-8.0% by weight of acetic acid and 0.01-0.3% by weight of a poorly-soluble-in-water solvent is particularly preferred. With an aqueous collecting agent containing less than 0.5% by weight of acrylic acid or less than 3.0% by weight of acetic acid, there is no improvement of acrylic acid collectability in the acrylic acid-collecting tower.
  • the acrylic acid concentration in the aqueous collecting agent is more than 5.0% by weight and/or the acetic acid concentration in the agent is more than 10.0% by weight, the monomer polymerization in the azeotropic distillation tower increases significantly and the long-term continuous operation of the apparatus becomes difficult and, in order to carry out the continuous operation, a large amount of a polymerization inhibitor is required, inviting poor economy.
  • the temperature at the top of the acrylic acid-collecting tower is preferably 50-70°C.
  • the aqueous collecting agent is generally fed into the acrylic acid-collecting tower 101 through a line 9 in the form of an aqueous solution prepared so as to have the above composition.
  • the aqueous phase separated in the storage tank 10 is circulated into the acrylic acid-collecting tower 101 through the line 2 and is used as the aqueous collecting agent.
  • the aqueous phase is circulated into the collecting tower 101 in an any desired proportion, preferably in a proportion of 50-90% by weight.
  • 50-90% by weight of the aqueous phase is circulated, the shortage of the collecting agent is made up with a fresh collecting agent through the line 9.
  • the aqueous acrylic acid solution formed in the collecting tower 101 is subjected to azeotropic distillation in the azeotropic distillation tower 102 in the presence of a poorly-soluble-in-water solvent.
  • the acrylic acid drawn out from the bottom of the azeotropic distillation tower 102 is sent to an esterification step through the line 7 and is used as a raw material for acrylic acid ester, per se or after the purification step.
  • the poorly-soluble-in-water solvent used as a solvent for azeotropic distillation in the present invention is a solvent having a solubility in water at room temperature, of 0.5% by weight or less, preferably 0.2% by weight or less.
  • the solvent is specifically at least one solvent selected from the group consisting of aliphatic hydrocarbons having 7-8 carbon atoms, aromatic hydrocarbons having 7-8 hydrocarbons and halogenated hydrocarbons having 2-6 carbon atoms.
  • the aliphatic hydrocarbons having 7-8 carbon atoms include heptane, heptene, cycloheptane, cycloheptene, cycloheptadiene, cycloheptatriene, methylcyclohexane, ethylcyclopentane, dimethylcyclohexane, ethylcyclohexane, etc.
  • the aromatic hydrocarbons having 7-8 carbon atoms include toluene, ethylbenzene, xylene, etc.
  • the halogenated hydrocarbons having 2-6 carbon atoms include tetrachloroethylene, trichloropropene, dichlorobutane, chloropentane, chlorohexane, chlorobenzene, etc.
  • Preferred as the poorly-soluble-in-water solvent is at least one solvent selected from the group consisting of heptane, dimethylcylohexane, ethylcyclohexane, toluene, ethylbenzene and xylene. More preferred is at least one solvent selected from the group consisting of heptane, toluene and ethylbenzene.
  • the present invention has the following meritorious effects.
  • Propylene was subjected to catalytic gas-phase oxidation with a molecular oxygen-containing gas in the presence of an oxidation catalyst to obtain a mixed gas containing 0.680 kg/h of acrylic acid, 0.014 kg/h of acetic acid and 0.450 kg/h of water.
  • An operation of collecting acrylic acid from the mixed gas was conducted using (1) an acrylic acid-collecting tower which was filled with cascade mini-rings (inside diameter: 14 mm) in a height of 6,000 mm and which was provided with a gas-releasing pipe at the top, a raw material-feeding pipe at the lower portion, and a bottom solution-drawing pipe at the bottom, and (2) an aqueous collecting agent containing 4.8% by weight of acrylic acid, 8.0% by weight of acetic acid and 0.01% by weight of octene.
  • Example 1 An operation of collecting acrylic acid from the mixed gas mentioned in Example 1 was conducted in the same manner as in Example 1 except that the aqueous collecting agent used in Example 1 was replaced by an aqueous solution containing 8.0% by weight of acetic acid but containing neither acrylic acid nor octene.
  • Example 1 An operation of collecting acrylic acid from the mixed gas mentioned in Example 1 was conducted in the same manner as in Example 1 except that the aqueous collecting agent used in Example 1 was replaced by an aqueous solution containing 4.8% by weight of acrylic acid but containing neither acetic acid nor octene.
  • the aqueous acrylic acid solution obtained in Example 1 as the bottom solution of the acrylic acid-collecting tower was introduced into an azeotropic distillation tower to conduct azeotropic distillation.
  • the azeotropic distillation tower had 60 sieve plates (plate-to-plate distance: 147 mm) and were provided with a distillate pipe at the top, a raw material-feeding pipe at the center and a bottom solution-drawing pipe at the bottom.
  • the azeotropic distillation was conducted using octene as a solvent for azeotropic distillation while controlling the tower top pressure at 140 mmHg, the reflux ratio (total moles of reflux per unit time/total moles of distillate per unit time) at 0.42, and the amount of raw material fed at 8.12 l/h.
  • the distillate from the top of the azeotropic distillation tower was introduced into a storage tank to separate it into an organic phase and an aqueous phase.
  • the aqueous phase contained 4.8% by weight of acrylic acid, 8.0% by weight of acetic acid and 0.01% by weight of octene.
  • the solution drawn out from the bottom of the azeotropic distillation tower contained 97.0% by weight of acrylic acid, 0.07% by weight of acetic acid, 0.02% by weight of water and 2.91% by weight of other substances.
  • the octene content in the solution was below the detection limit (1 ppm).
  • the above aqueous phase was circulated into the acrylic acid-collecting tower of Example 1 and used as an aqueous collecting agent.
  • an aqueous solution containing 0.674 kg/h of acrylic acid was obtained from the tower bottom and a gas containing 0.006 kg/h of acrylic acid was released from the tower top.
  • Example 1 An operation of collecting acrylic acid from the mixed gas mentioned in Example 1 was conducted in the same manner as in Example 1 except that the aqueous collecting agent used in Example 1 was replaced by an aqueous solution containing 4.2% by weight of acrylic acid, 8.2% by weight of acetic acid and 0.1% by weight of ethylbenzene.
  • Azeotropic distillation was conducted in the same manner as in Example 2 except that ethylbenzene was used as a solvent for azeotropic distillation and the reflux ratio was changed to 0.46. Also, acrylic acid collection in acrylic acid-collecting tower was conducted in the same manner as in Example 2.
  • the distillate from the top of the azeotropic distillation tower was introduced into a storage tank to separate it into an organic phase and an aqueous phase.
  • the aqueous phase contained 4.2% by weight of acrylic acid, 8.2% by weight of acetic acid and 0.1% by weight of ethylbenzene.
  • the solution drawn out from the bottom of the azeotropic distillation tower contained 97.2% by weight of acrylic acid, 0.06% by weight of acetic acid, 0.02% by weight of water and 2.72% by weight of other substances.
  • the ethylbenzene content in the solution was below the detection limit (1 ppm).
  • the above aqueous phase was circulated into the acrylic acid-collecting tower of Example 3 and used as an aqueous collecting agent.
  • an aqueous solution containing 0.675 kg/h of acrylic acid was obtained from the tower bottom and a gas containing 0.005 kg/h of acrylic acid was released from the tower top.
  • Example 1 An operation of collecting acrylic acid from the mixed gas mentioned in Example 1 was conducted in the same manner as in Example 1 except that the aqueous collecting agent used in Example 1 was replaced by an aqueous solution containing 3.2% by weight of acrylic acid, 7.9% by weight of acetic acid and 0.1% by weight of toluene.
  • Azeotropic distillation was conducted in the same manner as in Example 2 except that toluene was used as a solvent for azeotropic distillation and the reflux ratio was changed to 1.35. Also, acrylic acid collection in acrylic acid-collecting tower was conducted in the same manner as in Example 2.
  • the distillate from the top of the azeotropic distillation tower was introduced into a storage tank to separate it into an organic phase and an aqueous phase.
  • the aqueous phase contained 3.2% by weight of acrylic acid, 7.9% by weight of acetic acid and 0.1% by weight of toluene.
  • the solution drawn out from the bottom of the azeotropic distillation tower contained 97.5% by weight of acrylic acid, 0.03% by weight of acetic acid, 0.02% by weight of water and 2.45% by weight of other substances.
  • the toluene content in the solution was below the detection limit (1 ppm).
  • the above aqueous phase was circulated into the acrylic acid-collecting tower of Example 5 and used as an aqueous collecting agent.
  • an aqueous solution containing 0.673 kg/h of acrylic acid was obtained from the tower bottom and a gas containing 0.007 kg/h of acrylic acid was released from the tower top.
  • Example 1 An operation of collecting acrylic acid from the mixed gas mentioned in Example 1 was conducted in the same manner as in Example 1 except that the aqueous collecting agent used in Example 1 was replaced by an aqueous solution containing 1.8% by weight of acrylic acid, 7.5% by weight of acetic acid and 0.1% by weight of toluene.
  • Azeotropic distillation was conducted in the same manner as in Example 2 except that toluene was used as a solvent for azeotropic distillation and the reflux ratio was changed to 1.43. Also, acrylic acid collection in acrylic acid-collecting tower was conducted in the same manner as in Example 2.
  • the distillate from the top of the azeotropic distillation tower was introduced into a storage tank to separate it into an organic phase and an aqueous phase.
  • the aqueous phase contained 1.8% by weight of acrylic acid, 7.5% by weight of acetic acid, 0.1% by weight of toluene and 0.01% by weight of heptane.
  • the solution drawn out from the bottom of the azeotropic distillation tower contained 97.5% by weight of acrylic acid, 0.03% by weight of acetic acid, 0.02% by weight of water and 2.35% by weight of other substances.
  • the toluene content in the solution was below the detection limit (1 ppm).
  • the above aqueous phase was circulated into the acrylic acid-collecting tower of Example 7 and used as an aqueous collecting agent.
  • an aqueous solution containing 0.673 kg/h of acrylic acid was obtained from the tower bottom and a gas containing 0.007 kg/h of acrylic acid was released from the tower top.
  • Example 1 An operation of collecting acrylic acid from the mixed gas mentioned in Example 1 was conducted in the same manner as in Example 1 except that the aqueous collecting agent used in Example 1 was replaced by an aqueous solution containing 2.9% by weight of acrylic acid, 8.2% by weight of acetic acid, 0.1% by weight of ethylbenzene and 0.01% by weight of heptane.
  • the distillate from the top of the azeotropic distillation tower was introduced into a storage tank to separate it into an organic phase and an aqueous phase.
  • the aqueous phase contained 2.9% by weight of acrylic acid, 8.2% by weight of acetic acid, 0.1% by weight of ethylbenzene and 0.01% by weight of heptane.
  • the solution drawn out from the bottom of the azeotropic distillation tower contained 97.2% by weight of acrylic acid, 0.06% by weight of acetic acid, 0.02% by weight of water and 2.72% by weight of other substances.
  • the content of ethylbenzene and heptane in the solution was below the detection limit (1 ppm).
  • the above aqueous phase was circulated into the acrylic acid-collecting tower of Example 9 and used as an aqueous collecting agent.
  • an aqueous solution containing 0.674 kg/h of acrylic acid was obtained from the tower bottom and a gas containing 0.006 kg/h of acrylic acid was released from the tower top.
  • Example 1 An operation of collecting acrylic acid from the mixed gas mentioned in Example 1 was conducted in the same manner as in Example 1 except that the aqueous collecting agent used in Example 1 was replaced by an aqueous solution containing 1.5% by weight of acrylic acid, 7.9% by weight of acetic acid, 0.08% by weight of toluene and 0.01% by weight of heptane.
  • the distillate from the top of the azeotropic distillation tower was introduced into a storage tank to separate it into an organic phase and an aqueous phase.
  • the aqueous phase contained 1.5% by weight of acrylic acid, 7.9% by weight of acetic acid, 0.08% by weight of toluene and 0.01% by weight of heptane.
  • the solution drawn out from the bottom of the azeotropic distillation tower contained 97.5% by weight of acrylic acid, 0.05% by weight of acetic acid, 0.02% by weight of water and 2.43% by weight of other substances.
  • the content of toluene and heptane in the solution was below the detection limit (1 ppm).
  • the above aqueous phase was circulated into the acrylic acid-collecting tower of Example 11 and used as an aqueous collecting agent.
  • an aqueous solution containing 0.672 kg/h of acrylic acid was obtained from the tower bottom and a gas containing 0.008 kg/h of acrylic acid was released from the tower top.
  • Example 1 An operation of collecting acrylic acid from the mixed gas mentioned in Example 1 was conducted in the same manner as in Example 1 except that the aqueous collecting agent used in Example 1 was replaced by an aqueous solution containing 0.8% by weight of acrylic acid, 7.5% by weight of acetic acid, 0.07% by weight of toluene and 0.01% by weight of heptane.
  • the distillate from the top of the azeotropic distillation tower was introduced into a storage tank to separate it into an organic phase and an aqueous phase.
  • the aqueous phase contained 0.8% by weight of acrylic acid, 7.5% by weight of acetic acid, 0.07% by weight of toluene and 0.01% by weight of heptane.
  • the solution drawn out from the bottom of the azeotropic distillation tower contained 97.3% by weight of acrylic acid, 0.06% by weight of acetic acid, 0.02% by weight of water and 2.62% by weight of other substances.
  • the content of toluene and heptane in the solution was below the detection limit (1 ppm).
  • the above aqueous phase was circulated into the acrylic acid-collecting tower of Example 13 and used as an aqueous collecting agent.
  • an aqueous solution containing 0.672 kg/h of acrylic acid was obtained from the tower bottom and a gas containing 0.008 kg/h of acrylic acid was released from the tower top.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
EP96308837A 1995-12-05 1996-12-05 Verfahren zur Herstellung der Akrylsäure Expired - Lifetime EP0778255B1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP316182/95 1995-12-05
JP31618295 1995-12-05
JP7316182A JP3028925B2 (ja) 1995-12-05 1995-12-05 アクリル酸の製造方法

Publications (2)

Publication Number Publication Date
EP0778255A1 true EP0778255A1 (de) 1997-06-11
EP0778255B1 EP0778255B1 (de) 2000-05-10

Family

ID=18074215

Family Applications (1)

Application Number Title Priority Date Filing Date
EP96308837A Expired - Lifetime EP0778255B1 (de) 1995-12-05 1996-12-05 Verfahren zur Herstellung der Akrylsäure

Country Status (7)

Country Link
US (1) US5785821A (de)
EP (1) EP0778255B1 (de)
JP (1) JP3028925B2 (de)
KR (1) KR100336146B1 (de)
CN (1) CN1058701C (de)
DE (1) DE69608217T2 (de)
TW (1) TW397817B (de)

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998005398A1 (de) * 1996-08-05 1998-02-12 Basf Aktiengesellschaft Vorrichtung zur phasentrennung
US6180827B1 (en) 1998-02-03 2001-01-30 Hfm International, Inc. Recovery of acrylic acid from process or waste water streams
WO2003040079A1 (fr) * 2001-11-06 2003-05-15 Mitsubishi Chemical Corporation Procede d'extraction d'acide acrylique
EP1484310A2 (de) 2003-06-05 2004-12-08 Nippon Shokubai Co., Ltd. Verfahren zur Herstellung von Acrylsäure
US6958414B2 (en) 2002-12-16 2005-10-25 Basf Aktiengesellschaft Preparation of at least one organic compound by heterogeneously catalyzed partial gas-phase oxidation
US7196217B2 (en) 2003-08-06 2007-03-27 Basf Aktiengesellschaft Operation of a continuous heterogeneously catalyzed gas phase partial oxidation of at least one organic compound
CN1324057C (zh) * 2002-03-20 2007-07-04 株式会社日本触媒 制备聚丙烯酸的方法
US7294741B2 (en) 2001-12-14 2007-11-13 Stockhausen Gmbh Process for the production of acrylic acid
US7323590B2 (en) 2005-04-27 2008-01-29 Basf Aktiengesellschaft Process for rectificatively separating a liquid comprising acrylic acid and/or methacrylic acid
US7326323B2 (en) 2002-12-03 2008-02-05 Rohm And Haas Company High capacity purification of thermally unstable compounds
US7393436B2 (en) 2003-07-11 2008-07-01 Basf Aktiengesellschaft Thermal separating process for removing at least one stream containing enriched (meth) acrylic monomers
DE102008040799A1 (de) 2008-07-28 2008-12-11 Basf Se Verfahren zur Auftrennung von in einem Produktgasgemisch einer partiellen heterogen katalysierten Gasphasenoxidation einer C3-Vorläuferverbindung der Acrylsäure als Hauptbestandteil enthaltener Acrylsäure und als Nebenprodukt enthaltenem Glyoxal
DE102008041573A1 (de) 2008-08-26 2010-03-04 Basf Se Verfahren zur Auftrennung von in einem Produktgasgemisch einer partiellen heterogen katalysierten Gasphasenoxidation einer C3-Vorläuferverbindung der Acrylsäure als Hauptbestandteil enhaltener Acrylsäure und als Nebenprodukt enthaltenem Glyoxal
WO2012035019A1 (de) 2010-09-16 2012-03-22 Basf Se Verfahren zur herstellung von acrysläure aus ethanol und formaldehyd
WO2012034929A2 (de) 2010-09-16 2012-03-22 Basf Se Verfahren zur herstellung von acrylsäure aus methanol und essigsäure
WO2012045738A1 (de) 2010-10-08 2012-04-12 Basf Se Verfahren zur hemmung der unerwünschten radikalischen polymerisation von in einer flüssigen phase p befindlicher acrylsäure
US8299299B2 (en) 2008-07-28 2012-10-30 Basf Se Process for separating acrylic acid present as a main constituent and glyoxal present as a by-product in a product gas mixture of a partial heterogeneously catalyzed gas phase oxidation of a C3 precursor compound of acrylic acid
WO2014070735A1 (en) 2012-10-31 2014-05-08 Celanese International Corporation Integrated process for the production of acrylic acids and acrylates
WO2020020697A1 (de) 2018-07-26 2020-01-30 Basf Se Verfahren zur hemmung der unerwünschten radikalischen polymerisation von in einer flüssigen phase p befindlicher acrylsäure
WO2021191042A1 (de) 2020-03-26 2021-09-30 Basf Se Verfahren zur hemmung der unerwünschten radikalischen polymerisation von in einer flüssigen phase p befindlicher acrylsäure

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW553929B (en) * 1999-03-05 2003-09-21 Rohm & Haas Process for preparing (meth)acrylic acid
JP3948855B2 (ja) * 1999-06-10 2007-07-25 株式会社日本触媒 （メタ）アクリル酸の製造方法
US6500982B1 (en) 1999-06-28 2002-12-31 Rohm And Haas Company Process for preparing (meth) acrylic acid
JP4308372B2 (ja) 1999-07-06 2009-08-05 株式会社日本触媒 （メタ）アクリル酸および／または（メタ）アクロレインの吸収方法及びその装置
JP4615685B2 (ja) * 1999-08-23 2011-01-19 株式会社日本触媒 プレート式熱交換器の閉塞防止方法
US6566551B2 (en) 1999-12-02 2003-05-20 Nippon Shokubai Co., Ltd. Method for preventing effluent gas pipe from blocking
JP2001213839A (ja) 2000-02-03 2001-08-07 Nippon Shokubai Co Ltd （メタ）アクリル酸の製造方法
JP2001247510A (ja) 2000-03-08 2001-09-11 Nippon Shokubai Co Ltd アクリル酸の製造方法
ZA200209651B (en) 2001-12-10 2003-06-03 Nippon Catalytic Chem Ind Method and apparatus for absorbing (Meth)acrylic acid.
JP2003238485A (ja) * 2001-12-10 2003-08-27 Nippon Shokubai Co Ltd （メタ）アクリル酸の捕集方法および装置
US20030150705A1 (en) * 2002-01-08 2003-08-14 Deshpande Sanjeev D. Acrylic acid recovery utilizing ethyl acrylate and selected co-solvents
JP4440518B2 (ja) 2002-07-16 2010-03-24 株式会社日本触媒 アクリル酸の製造方法
JP3905810B2 (ja) * 2002-09-03 2007-04-18 株式会社日本触媒 アクリル酸製造プロセスにおける重合防止方法
CN1321968C (zh) * 2003-04-09 2007-06-20 上海华谊丙烯酸有限公司 共沸精馏提纯丙烯酸的方法
JP3999160B2 (ja) * 2003-05-14 2007-10-31 株式会社日本触媒 易重合性物質の製造方法
AU2004293262A1 (en) 2003-11-28 2005-06-09 Mitsubishi Chemical Corporation Method and apparatus for collecting (meth)acrolein or (meth)acrylic acid
JP4682599B2 (ja) * 2003-11-28 2011-05-11 三菱化学株式会社 （メタ）アクロレイン又は（メタ）アクリル酸の捕集方法及び捕集装置
JP4581395B2 (ja) 2003-12-24 2010-11-17 三菱化学株式会社 （メタ）アクリル酸の精製方法および（メタ）アクリル酸エステルの製造方法
KR100581766B1 (ko) * 2004-02-20 2006-05-22 주식회사 엘지화학 아크릴산의 제조 방법
JP2005247714A (ja) * 2004-03-02 2005-09-15 Mitsubishi Chemicals Corp （メタ）アクリル酸の製造方法
DE602005021361D1 (de) 2004-08-02 2010-07-01 Lg Chemical Ltd Verfahren zur herstellung von (meth)acrylsäure
CN1304354C (zh) * 2005-02-06 2007-03-14 蓝仁水 萃取与共沸精馏相结合提纯（甲基）丙烯酸的工艺方法
JP2009062289A (ja) * 2007-09-04 2009-03-26 Nippon Shokubai Co Ltd アクリル酸及び（メタ）アクリル酸エステルの製造方法
CN101835736B (zh) * 2007-10-23 2013-06-12 Lg化学株式会社 收集(甲基)丙烯酸的方法和收集(甲基)丙烯酸的装置
WO2014189829A1 (en) 2013-05-20 2014-11-27 Saudi Basic Industries Corporation Method for the purification of acetic acid and acrylic acid

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3429391A1 (de) * 1983-08-11 1985-02-21 Nippon Shokubai Kagaku Kogyo Co. Ltd., Osaka Verfahren zur herstellung von acrylsaeure

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3666632A (en) * 1968-10-08 1972-05-30 Asahi Chemical Ind Method for the separation of acrylic acid from aqueous solution containing acrylic acid and acetic acid
DE1965014A1 (de) * 1969-12-27 1971-07-01 Knapsack Ag Verfahren zur Abtrennung von Acrylsaeure aus waessriger Rohacrylsaeure
DE2005163A1 (de) * 1970-02-05 1971-08-19 Knapsack Ag, 5033 Knapsack Verfahren zur Abtrennung von Acrylsäure aus wäßriger Rohacrylsaure
US3855081A (en) * 1971-04-20 1974-12-17 Bp Chem Int Ltd Chemical process
NL180579C (nl) * 1972-05-24 1987-03-16 Sumitomo Chemical Co Werkwijze voor het scheiden van een mengsel bestaande uit acrylzuur, azijnzuur en water.
AR206439A1 (es) * 1974-10-07 1976-07-23 Celanese Corp Un metodo para la recuperacion de un acido acrilico crudo
JPS6054939B2 (ja) * 1977-08-04 1985-12-03 住友化学工業株式会社 粗製アクリル酸の精製方法
US4166774A (en) * 1977-12-05 1979-09-04 The Standard Oil Company Acrylic acid recovery and purification
TW295580B (de) * 1992-01-09 1997-01-11 Nippon Catalytic Chem Ind
JPH089567B2 (ja) * 1992-01-09 1996-01-31 株式会社日本触媒 アクリル酸製造においてアクリル酸を高純度に精製する方法

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3429391A1 (de) * 1983-08-11 1985-02-21 Nippon Shokubai Kagaku Kogyo Co. Ltd., Osaka Verfahren zur herstellung von acrylsaeure

Cited By (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1091387C (zh) * 1996-08-05 2002-09-25 巴斯福股份公司 相分离设备
WO1998005398A1 (de) * 1996-08-05 1998-02-12 Basf Aktiengesellschaft Vorrichtung zur phasentrennung
US6180827B1 (en) 1998-02-03 2001-01-30 Hfm International, Inc. Recovery of acrylic acid from process or waste water streams
WO2003040079A1 (fr) * 2001-11-06 2003-05-15 Mitsubishi Chemical Corporation Procede d'extraction d'acide acrylique
US7294741B2 (en) 2001-12-14 2007-11-13 Stockhausen Gmbh Process for the production of acrylic acid
CN1324057C (zh) * 2002-03-20 2007-07-04 株式会社日本触媒 制备聚丙烯酸的方法
US7326323B2 (en) 2002-12-03 2008-02-05 Rohm And Haas Company High capacity purification of thermally unstable compounds
US6958414B2 (en) 2002-12-16 2005-10-25 Basf Aktiengesellschaft Preparation of at least one organic compound by heterogeneously catalyzed partial gas-phase oxidation
EP1484310A2 (de) 2003-06-05 2004-12-08 Nippon Shokubai Co., Ltd. Verfahren zur Herstellung von Acrylsäure
EP1484310A3 (de) * 2003-06-05 2011-08-17 Nippon Shokubai Co., Ltd. Verfahren zur Herstellung von Acrylsäure
US7393436B2 (en) 2003-07-11 2008-07-01 Basf Aktiengesellschaft Thermal separating process for removing at least one stream containing enriched (meth) acrylic monomers
US7196217B2 (en) 2003-08-06 2007-03-27 Basf Aktiengesellschaft Operation of a continuous heterogeneously catalyzed gas phase partial oxidation of at least one organic compound
US7323590B2 (en) 2005-04-27 2008-01-29 Basf Aktiengesellschaft Process for rectificatively separating a liquid comprising acrylic acid and/or methacrylic acid
DE102008040799A1 (de) 2008-07-28 2008-12-11 Basf Se Verfahren zur Auftrennung von in einem Produktgasgemisch einer partiellen heterogen katalysierten Gasphasenoxidation einer C3-Vorläuferverbindung der Acrylsäure als Hauptbestandteil enthaltener Acrylsäure und als Nebenprodukt enthaltenem Glyoxal
US8299299B2 (en) 2008-07-28 2012-10-30 Basf Se Process for separating acrylic acid present as a main constituent and glyoxal present as a by-product in a product gas mixture of a partial heterogeneously catalyzed gas phase oxidation of a C3 precursor compound of acrylic acid
DE102008041573A1 (de) 2008-08-26 2010-03-04 Basf Se Verfahren zur Auftrennung von in einem Produktgasgemisch einer partiellen heterogen katalysierten Gasphasenoxidation einer C3-Vorläuferverbindung der Acrylsäure als Hauptbestandteil enhaltener Acrylsäure und als Nebenprodukt enthaltenem Glyoxal
WO2012035019A1 (de) 2010-09-16 2012-03-22 Basf Se Verfahren zur herstellung von acrysläure aus ethanol und formaldehyd
WO2012034929A2 (de) 2010-09-16 2012-03-22 Basf Se Verfahren zur herstellung von acrylsäure aus methanol und essigsäure
US8507721B2 (en) 2010-09-16 2013-08-13 Basf Se Process for preparing acrylic acid from ethanol and formaldehyde
US8877966B2 (en) 2010-09-16 2014-11-04 Basf Se Process for preparing acrylic acid from methanol and acetic acid
WO2012045738A1 (de) 2010-10-08 2012-04-12 Basf Se Verfahren zur hemmung der unerwünschten radikalischen polymerisation von in einer flüssigen phase p befindlicher acrylsäure
US9212122B2 (en) 2010-10-08 2015-12-15 Basf Se Process for inhibiting unwanted free-radical polymerization of acrylic acid present in a liquid phase P
WO2014070735A1 (en) 2012-10-31 2014-05-08 Celanese International Corporation Integrated process for the production of acrylic acids and acrylates
WO2020020697A1 (de) 2018-07-26 2020-01-30 Basf Se Verfahren zur hemmung der unerwünschten radikalischen polymerisation von in einer flüssigen phase p befindlicher acrylsäure
US11447439B2 (en) 2018-07-26 2022-09-20 Basf Se Method for inhibiting unwanted radical polymerisation of acrylic acid present in a liquid phase P
WO2021191042A1 (de) 2020-03-26 2021-09-30 Basf Se Verfahren zur hemmung der unerwünschten radikalischen polymerisation von in einer flüssigen phase p befindlicher acrylsäure

Also Published As

Publication number Publication date
US5785821A (en) 1998-07-28
TW397817B (en) 2000-07-11
KR970042465A (ko) 1997-07-24
JPH09157213A (ja) 1997-06-17
EP0778255B1 (de) 2000-05-10
DE69608217T2 (de) 2001-01-04
KR100336146B1 (ko) 2002-07-18
CN1154356A (zh) 1997-07-16
DE69608217D1 (de) 2000-06-15
CN1058701C (zh) 2000-11-22
JP3028925B2 (ja) 2000-04-04

Similar Documents

Publication Publication Date Title
US5785821A (en) Process for the production of acrylic acid
CN1264801C (zh) 甲醇羰基化反应生产乙酸工艺中脱除高锰酸盐降低化合物及烷基碘的方法
CN1572765B (zh) 从羧酸合成的母液中除去杂质的提取方法
CN100522916C (zh) 从甲醇羰基化工艺流中去除还原高锰酸盐的化合物
US5770765A (en) Process for the production of high-purity isophthalic acid
EP0882009B1 (de) Herstellung von aromatischen polycarbonsäuren
CN1572764A (zh) 从含水混合物中除去杂质的提取方法
KR101546464B1 (ko) (메트)아크릴산의 연속 회수 방법 및 회수 장치
JPH11503154A (ja) カルボニレーションプロセスの間に形成される希薄水性流よりの酢酸の回収
CN1572767A (zh) 从羧酸合成的母液中除去杂质的提取方法
CN101163658A (zh) 乙酸的制造方法
EP1035103B1 (de) Verfahren zur Herstellung von Acrylsäure
KR20050106355A (ko) 방향족 산의 제조 및/또는 정제 동안에 액체스트림으로부터 철 오염물을 제거하는 방법
JPH0684326B2 (ja) メタクロレインの回収方法
KR19980071856A (ko) 아크릴산의 회수 방법
JP4104232B2 (ja) 酢酸含有廃水からの酢酸回収方法
US6921830B2 (en) Method for purifying an organic solvent for the purposes of absorption of maleic acid anhydride
JP2003137833A (ja) テレフタル酸の製造方法
AU2003226883A1 (en) Method for the purification of acrolein
US6410753B2 (en) Process for producing trimellitic anhydride
JP3832868B2 (ja) アクリル酸の精製法
GB2096601A (en) Process for producing methacrylic acid
JPS6312460B2 (de)
JP2676910B2 (ja) 高純度０‐トルイル酸の製造法
US20090018361A1 (en) Process of producing high purity terephthalic acid

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): BE DE FR

17P Request for examination filed

Effective date: 19970710

17Q First examination report despatched

Effective date: 19990126

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): BE DE FR

REF Corresponds to:

Ref document number: 69608217

Country of ref document: DE

Date of ref document: 20000615

ET Fr: translation filed
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 20

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20151201

Year of fee payment: 20

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BE

Payment date: 20151207

Year of fee payment: 20

Ref country code: FR

Payment date: 20151110

Year of fee payment: 20

REG Reference to a national code

Ref country code: DE

Ref legal event code: R071

Ref document number: 69608217

Country of ref document: DE